Aspects of the present disclosure are generally directed to a system and method for reducing pressure in a pressurized chamber. More particularly, the system and method are directed to reducing intraocular pressure.
Glaucoma is a group of chronic optic nerve diseases and a leading cause of irreversible blindness. The major risk factor in glaucoma is elevated intraocular pressure due to improper drainage of aqueous humor from the eye. Reduction of intraocular pressure is the only proven treatment to stop the progression of vision loss by reducing stress on the optic nerve.
Standard glaucoma surgeries to reduce intraocular pressure, such as trabeculectomies and glaucoma drainage device implantation, tend to be lengthy and traumatic with unpredictable outcomes and complication rates of 20-60%. Implantable drainage devices function to drain excess aqueous humor from the eye, and installation of such a drainage device typically requires a surgical opening made in the sclera to reach the interior of the eye, in particular the anterior chamber or the posterior chamber. The drainage device is then inserted into the interior of the eye for conducting the aqueous humor to the subconjunctival space (with such a device herein referred to as a subconjunctival shunt), or externally of the conjunctiva (with such a device herein referred to as an external shunt).
A problem associated with subconjunctival shunts is potential scarring of the bleb in the subconjunctival space affecting its fibrous capsule formation around the outlet, which in many cases requires surgical revision that leads to additional risk of complications. Therefore, there is an ongoing search to identify and utilize alternate drainage sites to avoid many problems associated with bleb and fibrous capsule formations.
External shunts advantageously avoid bleb and fibrous capsule formation and the unpredictability of wound healing in the subconjunctival space. However, external shunts may not be capable of self-regulating or personalizing intraocular pressure. In certain cases, physicians may want to lower the intraocular pressure even further as one patient may cease vision loss with a pressure of 14 mmHg, while another patient may continue to lose vision with a pressure of 12 mmHg. Also, the pressure may increase over time due to clogging from proteins or other substances in the aqueous humor reducing permeability of the external shunt.
For the foregoing reasons there is a need for an improved system and method for reducing pressure in a pressurized chamber; specifically intraocular pressure.
The above and other needs are met by aspects of the present disclosure which, in one aspect, provides a system for reducing pressure. The system includes a pressure-reducing device including an inlet tubular member defining an inlet port, the inlet port being in communication with a central cavity defined by a housing and adapted to engage a pressurized chamber having a fluid therein, and an outlet tubular member having a distal end defining an outlet port, the outlet port being in communication with the central cavity via one or more channels defined by the outlet tubular member, the distal end of the outlet tubular member being adapted to extend to a surface external to the pressurized chamber, the pressure-reducing device receiving the fluid from the pressurized chamber via the inlet port and channeling the fluid to the surface external to the pressurized chamber via the central cavity and the outlet port. The system also includes a cutting tool configured to be capable of engaging the distal end of the outlet tubular member so as to adjust a length of the one or more channels defined by the outlet tubular member to regulate a pressure within the pressurized chamber, the length of the one or more channels being proportional to the flow resistance imparted to or the backpressure on a fluid flowing from the inlet port to the outlet port by at least the outlet tubular member.
In another aspect, a method for reducing pressure is provided. The method includes engaging an inlet port defined by an inlet tubular member of a pressure-reducing device with a pressurized chamber having a fluid therein, the pressure-reducing device comprising a central cavity defined by a housing, the central cavity being in communication with the inlet port, and including an outlet tubular member having a distal end defining an outlet port, the outlet port being in communication with the central cavity via one or more channels defined by the outlet tubular member, the distal end of the outlet tubular member extending to a surface external to the pressurized chamber, the pressure-reducing device being configured to receive the fluid from the pressurized chamber via the inlet port and to channel the fluid to the external surface via the central chamber and the outlet port. The method further includes adjusting a length of the one or more channels defined by the outlet tubular member to regulate a pressure within the pressurized chamber, the length of the one or more channels associated with the outlet tubular member being proportional to the flow resistance imparted to or the backpressure on the fluid flowing from the inlet port to the outlet port by at least the outlet tubular member.
These and other features, aspects, and advantages of the present disclosure will be apparent from a reading of the following detailed description together with the accompanying drawings, which are briefly described below. The present disclosure includes any combination of two, three, four, or more features or elements set forth in this disclosure or recited in any one or more of the claims, regardless of whether such features or elements are expressly combined or otherwise recited in a specific embodiment description or claim herein. This disclosure is intended to be read holistically such that any separable features or elements of the disclosure, in any of its aspects and embodiments, should be viewed as intended, namely to be combinable, unless the context of the disclosure clearly dictates otherwise.
For a more complete understanding of the present invention, reference should now be had to the embodiments shown in the accompanying drawings and described below. In the drawings:
The present disclosure now will be described more fully hereinafter with reference to the accompanying drawings, in which some, but not all aspects of the disclosure are shown. Indeed, the disclosure may be embodied in many different forms and should not be construed as limited to the aspects set forth herein; rather, these aspects are provided so that this disclosure will satisfy applicable legal requirements. Like numbers refer to like elements throughout.
Certain terminology is used herein for convenience only and is not to be taken as a limitation on the scope of the disclosure. For example, words such as “upper,” “lower,” “left,” “right,” “horizontal,” “vertical,” “upward,” and “downward” merely describe the configuration shown in the figures. Indeed, the components may be oriented in any direction and the terminology, therefore, should be understood as encompassing such variations unless specified otherwise.
The pressure-reducing device 100A generally comprises an inlet assembly 110 in communication with a central cavity 122 defined by a housing 120 and an outlet assembly 130 in communication with the central cavity 122. In some aspects, the inlet assembly 110 comprises an inlet tubular member 112 defining an inlet port 114. The inlet port 114 is adapted to engage a pressurized chamber (e.g., an anterior chamber of an eye) having fluid (e.g., aqueous humor) therein and thereby direct the fluid from the inlet port 114 to the central cavity 122. For example, in one instance, at least a portion of the inlet tubular member 112 of the pressure-reducing device 100A is implantable into the anterior chamber of an eye for draining aqueous humor therefrom. Representative configurations of such drainage devices of the general type disclosed herein are disclosed, for example, in U.S. Pat. No. 9,186,274 and U.S. Pat. No. 7,641,627, to Camras et al., each of which is incorporated herein by reference.
The inlet tubular member 112 of the pressure-reducing device 100A is substantially cylindrical and defines a hollow channel extending therethrough. As referenced throughout this description, a “channel” or “hollow channel” is one or more conduits defined by either the inlet tubular member 112 or an outlet tubular member 132A, 132B through a length thereof. The inlet tubular member 112 has a proximal end at which the inlet port 114 is defined and a distal end at which the inlet tubular member 112 is coupled to the central cavity 122. In some aspects, the proximal end of the inlet tubular member 112 is beveled or otherwise configured to facilitate entry of the proximal end of the inlet tubular member 112 into the pressurized chamber (e.g., the anterior chamber or other portion of the eye). In other aspects, the distal end of the inlet tubular member 112 defines a port that provides an outlet for fluid communication between the inlet tubular member 112 and the central cavity 122.
The hollow channel defined by the inlet tubular member 112 forms at least a portion of a flow path that permits the drainage of the fluid from the pressurized chamber to a surface external to the pressurized chamber. For example, the flow path permits drainage from the anterior chamber of the eye to a location or drainage site external to the anterior chamber. In this instance, the drainage site is an external ocular surface of the eye, such as the fornix or cul-de-sac region under the eyelid. In other instances, the drainage site includes another chamber within the eye, the subconjunctival space, the suprachoroidal space, or the like.
In some aspects, the inlet tubular member 112 has a length sufficient to provide the flow path between the pressurized chamber (e.g., the anterior chamber) and the external surface and to engage the housing 120 disposed on the external surface, thereby allowing the fluid to flow from the pressurized chamber through the hollow channel of the inlet tubular member 112 to the central cavity 122 defined by the housing 120. The fluid then flows from the central cavity 122 to an outlet tubular member 132A of the outlet assembly 130 and, in turn, to the external surface. For example, the aqueous humor is configured to flow from the anterior chamber of the eye through the inlet tubular member 112, through the central cavity 122 and the outlet assembly 130, and into the tear film associated with the eye when the pressure-reducing device 100A is implanted in or attached to the eye. For this purpose, the inlet tubular member 112 of the pressure-reducing device 100A has a minimum length, for example, of at least about 4 mm such that the housing 120 and outlet assembly 130 are positioned about the external surface (e.g., in the fornix or cul-de-sac region under the eyelid). In one aspect, the inlet tubular member 112 has a length of between about 4 mm and about 15 mm for adult humans. In other instances, the inlet tubular member 112 is provided in a standard length that is then cut to size by the surgeon prior to implantation. In use, in some aspects, the inlet tubular member 112 is implemented with the inlet port 114 being disposed in the pressurized chamber. For example, in use, the inlet tubular member 112 lies underneath the conjunctiva with the proximal end disposed in the anterior (or posterior) chamber of the eye. One skilled in the art will appreciate, however, that the dimensions and deployment location of the pressure-reducing device 100A varies considerably depending on the location to which the fluid drained from the pressurized chamber is directed.
In some aspects, an anchoring device or arrangement, such as one or more eyelet and/or bar is provided, adjacent the distal end of the inlet tubular member 112 and/or in engagement with the housing or head portion 120 of the pressure-reducing device 100A. For example, in one instance, the anchoring device comprises one or more eyelets 124 extending from a portion of an outer circumference of a first component of the housing 120A. In another example, one or more suture bars (not shown) extend from a portion of the outer surface of the inlet tubular member 112 or from an outer surface of the first component of the housing 120A. In these instances, the anchoring devices or arrangements are configured for contacting a surface external to the pressurized chamber (e.g., the sclera) when the pressure-reducing device 100A is implanted or engaged with, for example, the eye. More particularly, in this example, the one or more eyelets 124 are adapted for engaging the sclera and providing stability until and/or after biointegration of the inlet tubular member 112 and/or the housing/head portion 120 in the subconjunctival space.
In some aspects, a tab 128 is engageable with the outlet tubular member 132A (or outlet tube 132B,
In some aspects, a planar surface extending from the slideable engagement member of the tab 128 is configured to conform to the external surface (e.g., the external surface of the eye). In such aspects, the planar surface defines one or more holes through which the tab 128 can be sutured to the eye to position the outlet tubular member 132A. For example, as illustrated in
The housing 120 defines the central cavity 122. The first component of the housing 120A is integral with, or otherwise attached to, the distal end of the inlet tubular member 112 such that the central cavity 122 is in fluid communication with the flow path defined by the inlet tubular member 112 so as to receive a flow of the fluid therefrom. A second component of the housing 120B is integral with, or otherwise attached to, a proximal end of the outlet tubular member 132A such that the central cavity 122 is in fluid communication with a flow path defined by the outlet tubular member 132A and is able to direct fluid therethrough.
In the illustrated aspects, the inlet assembly 110 and the outlet assembly 130 are formed separately from the other and cooperate, when assembled, to define the housing 120 which encompasses the central cavity 122 within an interior thereof. A filter element 126, in some aspects, is provided between the first component of the housing 120A and the second component of the housing 120B. The filter element 126 aids to prevent bacterial migration into the pressurized chamber (i.e., the anterior or posterior chamber of the eye), depending on a size of the pores of the filter element 126, and, in some aspects, the filter element 126 provides resistance to outflow from the pressurized chamber. In other aspects (not illustrated), the inlet assembly 110, the housing 120, and the outlet assembly 130 are integrally formed, separately or in combination.
According to some aspects, the first and/or second component of the housing 120A/120B is dome-shaped (or convex) to provide a substantially continuous transition surface from along an outer surface of the housing 120 to the surface external to the pressurized chamber (e.g., the convex surface of the eye, where the housing 120 is configured to lie on the conjunctiva). Such a configuration/shape of the first and/or second component of the housing 120A/120B results in the pressure-reducing device 100A being better tolerated upon implantation. More particularly, in this instance, the pressure-reducing device 100A is better tolerated if the device itself does not feel like a foreign object in the eye in relation to the eyelid.
In other instances, the housing 120 is placed or lies subconjunctivally in a patient. More particularly, for example, one or more components of the pressure-reducing device (e.g., outlet tube 132A, 132B) is exposed subconjunctivally, a length of which is variable depending on a placement of the housing 120. In such instances, the filter element 126 is optional and central cavity size may be reduced. One skilled in the art will also appreciate that other shapes of the first and/or second component of the housing 120A, 120B are also suitable and appropriate for providing a similar sensory perception for the user. For example, in some instances, a minimally protruding, substantially flat first and/or second component of the housing 120A/120B with rounded edges is able to be equally well tolerated. Other appropriate designs are determinable by those skilled in the art. For example, in other instances, the plan view of the housing 120 is round or ovular (see, e.g.,
As disclosed herein, the first and second components of the housing 120A, 120B are configured to form, when assembled, the housing 120 having the central cavity 122 defined therein. The central cavity 122, in communication with the inlet tubular member 112, is thus configured to receive the fluid from the pressurized chamber through the inlet port 114 of the inlet tubular member 112. The fluid received by the central cavity 122 is then able to be drained from the central cavity 122 to a drainage site disposed distally to the central cavity 122. As such, in some instances, the pressure-reducing device 100A further comprises the outlet assembly 130 including the outlet tubular member 132A having a proximal end in communication with the central cavity 122 and a distal end defining an outlet port 134. In some aspects, the proximal end of the outlet tubular member 132A is engaged with the housing 120 independently of the inlet tubular member 112, such that the distal end of the outlet tubular member 132A is spaced apart from the proximal end of the inlet tubular member 112. That is, the outlet tubular member 132A is configured to be engaged with the housing 120 separately from the inlet tubular member 112. The outlet tubular member 132A is, in some aspects, in communication with the central cavity 122 via one or more channels defined thereby. More particularly, the one or more channels defined by the outlet tubular member 132A, in some instances, longitudinally extend between the distal end defining the outlet port 134 and the proximal end in communication with the central cavity 122. For example, the outlet tubular member 132A defining one channel, two channels, three channels, etc., is configured such that each of the defined channels longitudinally extend for a selected length, and are disposed between the distal end defining the outlet port 134 and the proximal end in communication with the central cavity 122. In this way, a flow path is defined by cooperation between the one or more channels of the outlet tubular member 132A, the central cavity 122, and the inlet tubular member 112, such that fluid directed therethrough is channeled outwardly from the outlet port 134 onto the external surface.
In some aspects, a transverse/lateral cross-sectional shape of the outlet tubular member 132A, is other than circular, and is another suitable shape such as, for example, oval, square, trapezoidal, rectangular, or any combination thereof. In these aspects, the channels defined by the outlet tubular member 132A are similarly or differently shaped relative to the transverse/lateral cross-sectional shape of the outlet tubular member 132A. For example, where the transverse/lateral cross-sectional shape of the outlet tubular member 132A is circular, the channels defined by the outlet tubular member 132A are semi-circular as divided by a membrane laterally extending through the interior of the outlet tubular member 132A.
Regardless of shape, the cross-sectional size of the outlet tubular member 132A and/or the one or more channels defined thereby, in some instances, varies to selectively alter the fluid flow characteristics of the fluid. For example, in some cases, the one or more channels comprise a relatively small cross-sectional area in order to restrict the fluid flow of the fluid due to, for example, friction. In one aspect, the cross-sectional inner diameter of the outlet tubular member 132A ranges, for example, from about 200 to about 800 micrometers, while each of the one or more channels defined by the outlet tubular member 132A comprises a cross-sectional inner diameter of between about 25 and about 100 micrometers.
In other aspects, a minimum length, of the outlet tubular member 132A is, for example, at least about 4 millimeters. More particularly, the outlet tubular member 132A has a length of between about 6 and about 30 millimeters for adult humans. In other instances, the outlet tubular member 132A is provided in a standard length that is then cut to size by the surgeon prior to implantation.
The outlet port 134 is adapted to extend from the housing 120 to the surface external to the pressurized chamber. That is, the distal end of the outlet tubular member 132A defining the port 134 is spaced apart from the housing 120, such that the one or more channels defined by the outlet tubular member 132A are configured to receive the fluid from the central cavity 122 through the proximal end thereof and direct the fluid through the one or more channels and out of the outlet port 134 to an external surface disposed distally to, externally to, or otherwise away from the pressurized chamber and the housing 120. Alternatively, the outlet port 134 is adapted to extend away from the surface external to the pressurized chamber.
In some aspects, the outlet tubular member 132A defines a single channel in communication with the central cavity 122 for directing the fluid through the outlet port 134 to the external surface. In other aspects, however, the outlet tubular member 132A is configured such that the channel is bifurcated along at least a portion of the outlet tubular member 132A to form two (or more) channels (see, e.g.,
More particularly, and as illustrated in
Accordingly, the pressure-reducing device 100A, 100B is configured for implantation in, for example, an eye, in order to direct fluid from the pressurized chamber (e.g., the anterior chamber) to a surface external thereto and thereby reduce pressure within the pressurized chamber. However, in some instances the implanted pressure-reducing device 100A, 100B requires adjustment or manipulation to further reduce, increase, or otherwise regulate the pressure within the pressurized chamber. For example, in some aspects, the pressure-reducing device 100A, 100B requires adjustment of a length of the one or more channels defined by the outlet tubular member 132A, 132B so as to regulate a pressure within the pressurized chamber. That is, the length of the one or more channels of the outlet tubular member 132A, 132B is proportional to the flow resistance imparted to or the backpressure on the fluid flowing from the inlet port 114 to the outlet port 134 by at least the outlet tubular member 132A, 132B. In other examples, the pressure-reducing device 100A, 100B requires adjustment of a cross-sectional area of the one or more channels defined by the outlet tubular member 132A, 132B, the cross-sectional area of the one or more channels of the outlet tubular member 132A, 132B also being proportional to the flow resistance imparted to or the backpressure on the fluid flowing from the inlet port 114 to the outlet port 134 by at least the outlet tubular member 132A, 132B. Other methods of manipulating the implanted pressure-reducing device 100A, 100B to further reduce or increase pressure include opening additional channels within the outlet tubular member 132A, 132B, removing lateral portions of the outlet tubular member 132A, 132B, occluding or obstructing one or more channels within the outlet tubular member 132A, 132B, etc.
In some aspects, and as illustrated in
In some aspects, the longitudinally extending tubular member 202 includes a valve 204 configured to open and close and, thereby, occlude or allow fluid flow along a flow path defined by the longitudinally extending tubular member 202 upon engagement with the outlet tubular member 132A. As illustrated in
In other aspects, the intraocular pressure or backpressure is measured by using tonometry or by creating a closed system and cannulating the outlet tubular member 132A with a pressure sensor. The pressure sensor may be contained in a fluid collection vial. When trying to assess the flow rate through the device an open system is created to allow fluid to fill over a certain period of time to assess volume (e.g., microliter) per time (e.g., a minute), and the like. Other methods and systems for measuring characteristics of the fluid relative to the pressure-reducing device 100A, 100B known to those of skill in the art are also contemplated.
Upon determining the backpressure on and/or the flow relative to the pressure-reducing device 100A, 100B, a determination is made as to whether the pressure-reducing device 100A, 100B should be adjusted or manipulated in order to reduce or increase the backpressure and/or flow resistance. Accordingly, and now referring to
In some aspects, the cutting tool 300 comprises a cut limiter 304 capable of engaging the distal end of the outlet tubular member 132A, 132B and a cutting element 306 spaced apart from the cut limiter 304 and capable of engaging the outlet tubular member 132A, 132B longitudinally therealong away from the distal end. Such a configuration, for example, limits an amount of the length of the outlet tubular member 132A, 132B (and thus the one or more channels defined thereby) that can be cut by the cutting tool 300 in one cut. For example, the cut limiter 304 and the cutting element 306 are arranged such that no more than about 1 millimeter in length is cut from the distal end of the outlet tubular member 132A, 132B.
In some aspects, the cutting tool 300 further comprises a guide element 308. For example, and as illustrated in
In some aspects, the cutting tool 400 further comprises a guide element 408. For example, and as illustrated in
Alternatively, for example, the actuator 402, upon actuation thereof, is configured to laterally move the cut limiter 404 into axial alignment with the guide element 408 substantially simultaneously with laterally moving the cutting element 406 to fully extend.
Now referring to
Generally, the insertion tools 500A-500C are configured to be capable of engaging the distal end of the outlet tubular member 132A, 132B so as to introduce an insert (see, e.g.,
In some aspects, the cannula 502A-502C is made of a compressible and flexible material, such that pressure from a user's hands along the longitudinal axis C-C of the cannula 502A-502C acts to introduce the insert into the one or more channels defined by the outlet tubular member. Otherwise, where the cannula 502A-502C comprises a trocar, an actuation mechanism engaged with the trocar acts to introduce the insert into the one or more channels defined by the outlet tubular member. Likewise, in some aspects, the cannula 502A-502C is configured to be withdrawn from the one or more channels defined by the outlet tubular member 132A, 132B substantially simultaneously with axially moving the insert along the cannula 502A-502C and through the distal end thereof to introduce the insert into the one or more channels defined by the outlet tubular member 132A, 132B. For example, the cannula 502A-502C is configured to be withdrawn from the one or more channels defined by the outlet tubular member 132A, 132B via suction applied to a proximal end of the cannula 502A-502C.
In other aspects, and referring to
The adapter mechanism 600 comprises, in some aspects, a longitudinally extending tubular body 602 having a proximal end defining a first port 604 configured to be engaged with a distal end of the outlet tubular member and an opposing distal end defining a second port 606. Thus, a flow path is defined between the first port 604 and the second port 606 of the adapter mechanism such that fluid, inserts, tools, etc., are introduceable through the second port 606 to the outlet port of the outlet tubular member by way of the first port 604. For example, an insertion tool (e.g., cannula 500A-500C,
In some aspects, and as illustrated in
In this manner, and referring to
In some aspects, the insert is configured to define one or more micro-channels extending axially between opposed longitudinal ends of the insert. As used herein, a “micro-channel” refers specifically to one or more longitudinal grooves, bores, chamfers, etc., extending axially between opposed longitudinal ends of the insert. As one of ordinary skill in the art understands, the more micro-channels that are formed within the insert, the more that flow resistance will decrease, such that backpressure is reduced. For example, in
In another example, in
In another example, in
In a still further example, in
The insert 700D comprises, in some instances, a bore or hole 704 defined laterally through the circumferential surface of the outlet tubular member 132A and through a circumferential surface of the insert 700D, is an alternative to adjusting a length of the outlet tubular member 132A, for example, by cutting. In other aspects, more than one bore 704 is configured to be formed in the insert 700D.
In some aspects, a limiting region 808 is defined about the body portion 802 towards an end of the body portion 802 at which the guide element 806 is provided. The limiting region 808 is configured as a mechanism to prevent the boring element 804 from over-extending along the longitudinal axis of the body portion 802. Accordingly, the bore tool 800 is configured to form an outlet port supplemental to the outlet port 134 as illustrated in
In some aspects, where an insert 700A-D is inserted within the outlet tubular member 132A, such as those provided in
In some aspects, a cross-sectional area of the one or more channels of the outlet tubular member 132A, 132B is configured to be reduced by a compression tool.
In other aspects, compression is achievable by tying a suture (not shown) about the sheath 900 or about the outlet tubular member 132, directly. For example, a suture is usable to extend around the circumferential surface of the outlet tubular member at least one time and subsequently be tightened so as to reduce the cross-sectional area of the one or more channels. Accordingly, the reduced cross-sectional area of the outlet tubular member increases the flow resistance imparted to the fluid or the backpressure on the fluid. The suture is capable, in some aspects, of being removed (e.g., cut) from the outlet tubular member in order to return the cross-sectional area of the one or more channels defined by the outlet tubular member to a previous, non-compressed state.
In some aspects, flow resistance and/or pressure is able to be adjusted by opening or occluding one or more of the channels of the outlet tubular member. For example, for an outlet tubular member defining multiple channels will have a proportional relationship to the number of channels opened and the pressure reduction based on the decrease in flow resistance. Likewise, for example, for an outlet tubular member defining two or more channels (e.g., outlet tubular member 132B,
Accordingly,
In
In
In
In
Referring now to
In some aspects, the loop member 1106 extends from the proximal end thereof to a distal end comprising an inclined surface 1108 extending at an obtuse angle away from the proximal end of the loop member 1106. Accordingly, in such instances, the obtuse angle at which the inclined surface 1108 of the loop member 1106 extends from the proximal end thereof corresponds to a curvature of the surface external to the pressurized chamber. For example, the inclined surface 1108 of the loop member 1106 corresponds to the curvature of an eye in which the pressure-reducing device 100A, 100B is implanted.
In some aspects, the loop arrangement 1204 includes an adjustable loop member 1206 having a proximal end extending from the first end of the shaft 1202 to an opposed distal end. The adjustable loop member 1206 defines a loop that is configured to receive the outlet tubular member 132A, 132B through a central portion defined by the adjustable loop member 1206. In some aspects, the adjustable loop member 1206 is coupled to an adjustment arrangement 1208 engaged between the shaft 1202 and the proximal end of the adjustable loop member 1206.
More particularly, the adjustment arrangement 1208 is configured to extend or retract the proximal end of the adjustable loop member 1206 with respect to the shaft 1202 so as to alter a size of a loop defined by the adjustable loop member 1206 and to release or secure the distal end of the outlet tubular member 132A, 132B therein. Moving the adjustment arrangement 1208 axially about a longitudinal axis E-E of the shaft 1202 enables retraction and extension of the adjustable loop member 1206.
For example,
In another example,
In some aspects, the loop arrangement 1304 includes an adjustable loop member 1306 having a proximal end extending from the first end of the shaft 1302 to an opposed distal end. The adjustable loop member 1306 defines a loop that is configured to receive the outlet tubular member 132A, 132B through a central portion defined by the adjustable loop member 1306. As illustrated in
In some aspects, the adjustable loop member 1306 is coupled to an adjustment arrangement 1312 engaged between the shaft 1302 and the proximal end of the adjustable loop member 1306. More particularly, the adjustment arrangement 1312 is configured to extend or retract the proximal end of the adjustable loop member 1306 with respect to the shaft 1302 and the fixed loop member 1308 so as to alter a size of a loop defined by the adjustable loop member 1306 and to release or secure the distal end of the outlet tubular member 132A, 132B therein. Moving the adjustment arrangement 1312 axially along a longitudinal axis F-F of the shaft 1302 enables retraction and extension of the adjustable loop member 1306.
For example,
In another example,
As illustrated in
Embodiments of a manipulation tool other than those described above in reference to
Referring now to
In step 1602, an inlet port defined by an inlet tubular member of a pressure-reducing device is engaged with a pressurized chamber having a fluid therein, the pressure-reducing device comprising a central cavity defined by a housing, the central cavity being in communication with the inlet port, and comprising an outlet tubular member having a distal end defining an outlet port, the outlet port being in communication with the central cavity via one or more channels defined by the outlet tubular member, the distal end of the outlet tubular member extending to a surface external to the pressurized chamber, the pressure-reducing device being configured to receive the fluid from the pressurized chamber via the inlet port and to channel the fluid to the external surface via the central chamber and the outlet port.
In step 1604, the length, constriction, opening, and/or obstruction of the one or more channels defined by the outlet tubular member is adjusted to regulate a pressure within the pressurized chamber, the length of the one or more channels associated with the outlet tubular member being proportional to the flow resistance imparted to or the backpressure on the fluid flowing from the inlet port to the outlet port by at least the outlet tubular member.
Many modifications and other aspects of the disclosure will come to mind to one skilled in the art to which this disclosure pertains having the benefit of the teachings presented in the foregoing descriptions and the associated drawings. Therefore, it is to be understood that the disclosure is not to be limited to the specific aspects disclosed herein and that modifications and other aspects are intended to be included within the scope of the appended claims. Although specific terms are employed herein, they are used in a generic and descriptive sense only and not for purposes of limitation.